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BacLink 3.laboratory Information Systems

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0% found this document useful (0 votes)
52 views8 pages

BacLink 3.laboratory Information Systems

Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd
You are on page 1/ 8

BacLink

Laboratory Information Systems

WHO Collaborating Centre for


Surveillance of Antimicrobial Resistance

Boston, July 2022


BacLink and Laboratory information systems

The purpose of this document is to describe to IT staff the purpose of the WHONET
and BacLink softwares, and how they may be useful to the laboratory staff,
clinicians, pharmacists, and infection control staff in your institution. The document
also provides instructions to IT staff on what laboratory staff will need to implement
WHONET and BacLink.

The document covers the following areas:


Part 1. What are WHONET and BacLink?
Part 2. What does the laboratory need from the IT Department to run
WHONET?
Part 3. What information should be in the export file?
Part 4. How should the information be organized?
Part 5. How often should data be exported?
Part 6. What comes next?

Part 1. What are WHONET and BacLink?

WHONET is a free Windows-based desktop application developed by the WHO


Collaborating Centre for Surveillance of Antimicrobial Resistance for the laboratory-
based surveillance of infectious diseases and antimicrobial resistance.

The principal goals of the software are:


• to enhance capabilities for analyzing laboratory data; and
• to promote national and international collaboration through the exchange of data.

The software is used in over 130 countries around the world managing data from
over 2300 clinical, public health, veterinary, and food laboratories. WHONET can be
used by individual laboratories or as part of national and international surveillance
networks.

Many laboratories around the world already have well-established computer


databases that meet the day-to-day needs of clinical reporting, specimen processing,
and long-term data storage. Unfortunately, most of these systems have limited
capacity for sophisticated data analysis. It is in these areas that WHONET is a
valuable supplement to existing systems.

This purpose of the BacLink software is the conversion and standardization of


microbiology data from existing systems into WHONET. You can convert data on a
weekly, monthly, or ad hoc basis, or in a number of institutions, it has also been
possible to automate and schedule the entire process. Both WHONET and BacLink,
available in 44 languages, can be downloaded from the WHONET website:
https://whonet.org.

By converting data to WHONET, laboratories have the benefits of: 1. flexible data
analysis capabilities; and 2. the ability to share data with other laboratories, for
example in a national surveillance network.
Part 2 – What does the laboratory need from the IT Department to run
WHONET?

Since BacLink cannot access the internal databases of your laboratory information
system (LIS), the laboratory needs a data file exported from your system with the
desired patient information and microbiological results. In many institutions, the
most convenient type of file to create is a simple delimited text file, though BacLink
can also accept a number of other formats. Information to be included in this export
is suggested in Part 3, and the organization of the data in the file is discussed in Part
4.

Fortunately, most information systems do have the capability of creating such text
files using existing data export, report, or interface options. In the case of the
following systems, we have prepared detailed instructions and report templates that
you should be able to apply directly:
– Meditech Magic
– Cerner Classic

It is also possible to convert data from the following systems, but we have not
developed formal documentation describing the process. For further details, please
contact us directly.
– ADBakt (Sweden, Denmark)
– MADS (Denmark)
– Oman Health Information System (Oman)
– WinPath (Malaysia)

If you do not have any of the systems indicated above, then you should try to create
a delimited text file with the information described below.

Our group is currently working on the development of interface options for Meditech
Client/Server, Cerner Millenium, and Mysis. If you would like to assist in the
development or testing of interfaces for these systems or any other system, please
contact John Stelling at [email protected].

Part 3. What information should be in the export file?

Data fields

The following is a list of suggested data fields to be included in the export. The
precise list should be discussed with laboratory staff, and should reflect the
information available in your system and the data analysis needs of clinical staff. All
of the fields are optional, though a few are highly recommended. Feel free to delete
any fields which are unneeded and add additional fields that you desire.

Patient fields:
Identification number (e.g. Medical record number) – recommended
Patient first name and last name or Patient full name
Sex
Date of birth and/or age
Date of admission

Location fields
Patient location (ward or clinic) – recommended
Department or specialty
Institution or facility (in the case of a laboratory serving multiple institutions)
Type of location (for example, inpatient or outpatient)

Specimen fields
Specimen or accession number – recommended
Specimen collection date – recommended
Specimen type (blood, urine, cerebrospinal fluid, etc.) – recommended

Organism results
Organism – recommended
Antimicrobial susceptibility test results – recommended

Most of the above fields are self-explanatory. For antimicrobial susceptibility test
results, a few additional comments are needed.

The three most common methods for performing antimicrobial susceptibility tests
are:
1. Disk diffusion, also known as Kirby-Bauer. Results are measured in millimeters.
2. MIC determination. MIC = minimal inhibitory concentration. In routine
laboratories, MICs are usually determined with automated susceptibility test
instruments, such as MicroScan, Sensititre, and Vitek. Quantitative results
are given in the form of a concentration, for example micrograms/milliliter
(µg/ml).
3. Etest. This is a specialized version of a MIC test. It is a more expensive test
than routine MIC tests. Results are also measured as concentrations, for
example (µg/ml).

Laboratories may perform one, two, or all three of these methods. Some
laboratories enter the quantitative test measurements directly into the computer
system (millimeters or µg/ml) or the test interpretation (resistant, intermediate, or
susceptible) or both. Examples of how you could export the antibiotic results are
provided in Part 4.

There are some additional specialized antibiotic tests that you should also to try to
export if feasible: beta-lactamase, ESBL, Dtest, etc. In many computer systems,
these tests are treated in the same way as other antimicrobial tests, so no special
handling is required to capture the results. In other systems, results are saved
internally in a separate field that you should try to capture.

Data codes and date formats

BacLink has a flexible interface for mapping data codes and date formats. So you
should export whatever codes and values are most convenient for you and your
laboratory staff. If you have the choice between exporting a data code (e.g. UR) or
the corresponding full text (URINE), the full text will probably be more convenient for
the users who will do the code mapping.What specimens should be included in
the export file?

When you export results from your LIS, you can export results from all specimens or
from a subset of specimens. The three most common options would be:

1. All specimens
2. All “positive” specimens (do not include specimens with “No growth”)
3. All “positive” specimens with antimicrobial susceptibility test results

Any of these approaches are reasonable options. The first approach will have the
most information available for analysis, but these files can also be very large
because of the large number of “negative” results. Option 2 is a reasonable
compromise for many laboratories between the value of the information, the size of
the data file, and the speed of data analysis.

Part 4. How should the information be organized?

File format

Most institutions find the use of delimited text files to be the most convenient means
of exporting data to WHONET. The choice of field delimiter (comma, tab, semi-
colon, etc.) is configurable by the user. Other options include fixed-column text,
Microsoft Access, or dBASE. The use of a file header (the first row of the file
indicates the names of the data fields) is often convenient for the data manager, but
is not a requirement.

BacLink works with “flat” non-relational databases. Create one column for each of
the fields that you intend to export: medical record number, patient location,
collection date, organism, etc.

Antibiotic results – organization of records

Because each bacterial isolate is usually tested against multiple antibiotics and
perhaps by one than one test method, there are a few possible acceptable ways of
organizing your antibiotic test results in the export file. The two most common
variations are described below. You should decide which of these two approaches
would be easiest to implement and maintain in your system.

1. One isolate per row: Each row in the export file corresponds to the results from
one organism. All results from this organism are saved in this one record.
People entering data manually into Excel usually organize their data in this way –
with all of the antibiotic results for one organism saved as part of the same
record/data row. Some hospital systems also export data in this way.

Example:
First name, Last name, Sex, Location, Specimen type, Specimen date, Organism, PEN, ERY, VAN
John, Smith, Male, Neurology, Blood, 1/1/2006, S. aureus, R, R, S
Mary, Jones, Female, Nursery, CSF, 3/10/2006, S. pneumoniae, S, S, S
Tom, Brown, Male, ICU, Wound, 5/8/2006, C. albicans

The last record illustrates an isolate in which no antibiotics were tested.

2. One antibiotic result per row: Each row in the export file corresponds to one
antibiotic test result. So if an organism is tested against 12 antibiotics, this
organism would require 12 records in the export file. This approach is very
commonly used when exporting data from relational databases, such as those
common in LIS softwares or laboratory instruments.
Example
First name, Last name, Sex, Location, Specimen type, Specimen date, Organism, Antibiotic, Result
John, Smith, Male, Neurology, Blood, 1/1/2006, S. aureus, PEN, R
John, Smith, Male, Neurology, Blood, 1/1/2006, S. aureus, ERY, R
John, Smith, Male, Neurology, Blood, 1/1/2006, S. aureus, VAN, S
Mary, Jones, Female, Nursery, CSF, 3/10/2006, S. pneumo, PEN, S
Mary, Jones, Female, Nursery, CSF, 3/10/2006, S. pneumo, ERY, S
Mary, Jones, Female, Nursery, CSF, 3/10/2006, S. pneumo, VAN, S
Tom, Brown, Male, ICU, Wound, 5/8/2006, C. albicans

In this scenario, BacLink processes one block of records at a time, so it is important


that all of the antibiotics from one isolate be stored sequentially together into the
same block. With exports from relational databases, this often happens correctly
as the default behavior, but if this doesn’t happen then the data manager should
introduce a “sorting” step to ensure that the antibiotics of one isolate are stored
together.

An advantage of the first approach is that files are much smaller in size; these files
are also easy to manage in Excel and other data management softwares. An
advantage of the second approach is that it is often easier to maintain in the long-
term as additional antibiotics are added to the database. If the laboratory starts
testing a new antibiotic, the first approach would require the programmer to add new
columns to the data export, and if this is not done, the new antibiotic will not be
captured. In the second approach, new antibiotics will generally show up
automatically as additional rows in the export file, requiring no change in the
structure of the data file.

Antibiotic results – test measurements and test interpretations

As mentioned above, it is possible to export test measurements (mm or µg/ml), test


interpretations (resistant, intermediate, or susceptible), or both to the export files. If
you have both, you should export both if possible. If you must decide between the
two, the measurement is more valuable since the interpretation can be deduced from
the measurement.

Example with disk diffusion data – exporting the measurement and the interpretation
First name, Last name, Specimen type, Specimen date, Organism, Antibiotic, Measurement, Interp.
John, Smith, Blood, 1/1/2006, S. aureus, PEN, 6, R
John, Smith, Blood, 1/1/2006, S. aureus, ERY, 10, R
John, Smith, Blood, 1/1/2006, S. aureus, VAN, 19, S
Example with MIC data – exporting the measurement and the interpretation
First name, Last name, Specimen type, Specimen date, Organism, Antibiotic, Measurement, Interp.
Mary, Jones, CSF, 3/10/2006, S. pneumo, PEN, 0.064, S
Mary, Jones, CSF, 3/10/2006, S. pneumo, ERY, <=0.25, S
Mary, Jones, CSF, 3/10/2006, S. pneumo, VAN, 1, S

Antibiotic results – test methods

If your laboratory only uses one test method, then there is no need for you to indicate
the test method in the exported data file, as in the examples given above. On the
other hand, if your laboratory does testing by more than one method, then you
should also try to indicate the test method in the exported data file.

Example with disk and MIC data


First name, Last name, Specimen type, Specimen date, Organism, Antibiotic, Method, Measurement,
Interp.
John, Smith, Blood, 1/1/2006, S. aureus, Disk, PEN, 6, R
John, Smith, Blood, 1/1/2006, S. aureus, Disk, ERY, 10, R
John, Smith, Blood, 1/1/2006, S. aureus, Disk, VAN, 19, S
Mary, Jones, CSF, 3/10/2006, S. pneumo, MIC, PEN, 0.064, S
Mary, Jones, CSF, 3/10/2006, S. pneumo, MIC, ERY, <=0.25, S
Mary, Jones, CSF, 3/10/2006, S. pneumo, MIC, VAN, 1, S
Tom, Brown, Wound, 5/8/2006, C. albicans

For many laboratories, this last example presented could be a useful model to
emulate when you develop your export routine. In addition to the fields shown in this
example, you should also export the other relevant fields described earlier.

Part 5. How often should data be exported?

The frequency of data exports will depend on how often the laboratory staff would
like to update their databases for analysis. If the focus is only on general trends in
infection and resistance, then once a quarter or once a year may be adequate.
However, if there is interest in tying data analysis to prompt outbreak detection and
isolate alerts, then a monthly or weekly export would be more appropriate.

An automated daily download and analysis would be the ideal solution. This has
been implemented in a few institutions, and we are currently working on interface
tools to make this a more viable option for laboratories, but at the present time, most
laboratories accomplish the data conversions and analyses interactively on a weekly,
monthly, or quarterly basis.

For information on the use of BacLink in automated batch mode, please contact us
directly for details at [email protected].

Part 6. What comes next?

If you succeed in creating a text file with the information described above, the next
step is to use BacLink to convert the text file to the WHONET data format. This can
be accomplished by the IT Department, by the laboratory, or by both groups in
collaboration. For information on how to get started with BacLink, continue with the
tutorial on “BacLink – Getting started”.

If you have any questions about BacLink or WHONET, feel free to contact us at
[email protected]. If you would like to assist us in the development of
additional interface options for BacLink, we would also be very glad to hear from you.

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